Deacetylation of Miro1 by HDAC6 blocks mitochondrial transport and mediates axon growth inhibition

Author:

Kalinski Ashley L.12ORCID,Kar Amar N.3ORCID,Craver John3,Tosolini Andrew P.4ORCID,Sleigh James N.45ORCID,Lee Seung Joon3,Hawthorne Alicia6,Brito-Vargas Paul3,Miller-Randolph Sharmina3,Passino Ryan2,Shi Liang3ORCID,Wong Victor S.C.7,Picci Cristina7,Smith Deanna S.3ORCID,Willis Dianna E.7ORCID,Havton Leif A.8,Schiavo Giampietro459ORCID,Giger Roman J.2ORCID,Langley Brett7,Twiss Jeffery L.3ORCID

Affiliation:

1. Department of Biology, Drexel University, Philadelphia, PA

2. Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, MI

3. Department of Biological Sciences, University of South Carolina, Columbia, SC

4. Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, UK

5. UK Dementia Research Institute, University College London, London, UK

6. Department of Cell Biology, Emory University, Atlanta, GA

7. Burke Neurological Institute, White Plains, NY

8. Departments of Neurology and Neurobiology, University of California, Los Angeles, Los Angeles, CA

9. Discoveries Centre for Regenerative and Precision Medicine, University College London Campus, London, UK

Abstract

Inhibition of histone deacetylase 6 (HDAC6) was shown to support axon growth on the nonpermissive substrates myelin-associated glycoprotein (MAG) and chondroitin sulfate proteoglycans (CSPGs). Though HDAC6 deacetylates α-tubulin, we find that another HDAC6 substrate contributes to this axon growth failure. HDAC6 is known to impact transport of mitochondria, and we show that mitochondria accumulate in distal axons after HDAC6 inhibition. Miro and Milton proteins link mitochondria to motor proteins for axon transport. Exposing neurons to MAG and CSPGs decreases acetylation of Miro1 on Lysine 105 (K105) and decreases axonal mitochondrial transport. HDAC6 inhibition increases acetylated Miro1 in axons, and acetyl-mimetic Miro1 K105Q prevents CSPG-dependent decreases in mitochondrial transport and axon growth. MAG- and CSPG-dependent deacetylation of Miro1 requires RhoA/ROCK activation and downstream intracellular Ca2+ increase, and Miro1 K105Q prevents the decrease in axonal mitochondria seen with activated RhoA and elevated Ca2+. These data point to HDAC6-dependent deacetylation of Miro1 as a mediator of axon growth inhibition through decreased mitochondrial transport.

Funder

National Institutes of Health

Wellcome Trust

Horizon 2020 Framework Programme

UK Dementia Research Institute Foundation

Dr. Miriam and Sheldon G. Adelson Medical Research Foundation

South Carolina Experimental Program to Stimulate Competitive Research and Institutional Development Awards Program

Office of the Vice President for Research, University of South Carolina

Publisher

Rockefeller University Press

Subject

Cell Biology

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